CVS Feminine Intimate Powder

Manufacturer
PureTek Corporation
Effective date
2020-03-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:38:36

Label at a glance#

ProductCVS Feminine Intimate Powder
Active ingredientMICONAZOLE NITRATE
Label structure8 sections

Indications and uses

for the treatment and relief of external genital itching relieves itching, scaling, cracking, burning, redness, soreness, irritation, discomfort and chafing associated with external genital itching

Dosage and administration

clean the affected area and dry thoroughly  apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor  supervise children in the use of this product 

Storage and handling

store between 59°-86°F lightly shake bottle to loosen settled powder

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient
Miconazole Nitrate 2%

Purposes

OTC - PURPOSE SECTION

Antifungal 

Uses

INDICATIONS & USAGE SECTION

  • for the treatment and relief of external genital itching
  • relieves itching, scaling, cracking, burning, redness, soreness, irritation, discomfort and chafing associated with external genital itching

Warnings

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on children under 2 years of age unless directed by a doctor.

OTC - WHEN USING SECTION

When using this product avoid contact with the eyes.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation occurs or if there is no improvement within 2 weeks

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • clean the affected area and dry thoroughly 
  • apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor 
  • supervise children in the use of this product 

Other information

STORAGE AND HANDLING SECTION

  • store between 59°-86°F
  • lightly shake bottle to loosen settled powder

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aleurites Moluccana Seed Oil, Aloe Barbadensis (Aloe Vera) Leaf Juice Powder, Bisabolol, Carthamus Tinctorius (Safflower) Oleosomes, Fragrance, Nylon-12, Silica, Sodium Benzoate, Sodium Hyaluronate, Zea Mays (Corn) Starch, Zingiber Officinale (Ginger) Root Extract.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANELPACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59088-24459088-244-07

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2a956e5b-fcf8-3e5a-e063-6294a90a7be9eda5026e-d941-4fb8-a0c6-c70ea1d685322024-12-31WarningsExact identifier
spl set id: eda5026e-d941-4fb8-a0c6-c70ea1d68532

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.